Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Dishes And Silverware


nw0528

Recommended Posts

nw0528 Apprentice

I'm new here and had not realized people actually replace kitchen items when diagnosed with celiac disease. I understand about Teflon pans. I'm wondering if dishes and silverware are believed to be safe from cross contamination if they are put in the dishwaher. People talked about not using the same toaster, colander, pots and pans...but what about for things you put in your dishwasher?

Thanks!

Nicole


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



psawyer Proficient

Welcome aboard.

We are now completely gluten-free, but for many years we had a mixed kitchen. We put everything into the dishwasher, and treated it as safe when it came out.

Things to be concerned about are those that are porous or scratched. Wooden spoons are the biggest item, but scratched non-stick pans and scratched plastic utensils or dishes are also a concern. The screen on a metal colander is problematic. You can not possibly clean all of the crumbs out of a toaster--get a new one.

cattriona Newbie

do you have a severe reaction to gluten? the toaster is probably a good idea, but if you don't have a sever allergy, as long as everything is washed properly, then it should be ok. never been a problem for myself or any of the other celiac sufferers i know

YoloGx Rookie

Am wondering if an old aluminum pressure cooker should be replaced. I used it as a regular pot to cook soup in and wonder if it "extended" my congestion so to speak. I have rarely used it otherwise. Am considering throwing it out.

Bea

wschmucks Contributor

All of my dishes, cookware etc is all seperate from my gluten eating roomate. We dont have a dish washer, so i just dont feel like its a good idea (we even use seperate sponges). I knew that if i didnt do that, every time i would get sick I would wonder if it was from the dishes. I just bought myself three dishes, bowls, sets of silver ware, and it was that big of a deal.

Thing you really NEED to replace are those listed above, toaster, wooden spoons (just switch to metal), any teflon surface (i just switched to aluminum pots/ pans), wooden cuting boards, and do a VERY thorough cleaning of the shelves and fridge. I would recommend keeping your food on one side of the kitchen and making it a habit it put down your gluten-free cutting board when you place any of your food on the counter. Even if you arent sensetive, if you have Celiac the external results are not the same as the internal-- meaning it might not be making you feel sick, but its still attacking your intestines.

Bea-- I have an aluminum pressure cooker too-- I think we should be ok with aluminum as long as there is no teflon. I havent used mine yet, but my impression was as long as it is a pure metal surface we should be good to go.

YoloGx Rookie
All of my dishes, cookware etc is all seperate from my gluten eating roomate. We dont have a dish washer, so i just dont feel like its a good idea (we even use seperate sponges). I knew that if i didnt do that, every time i would get sick I would wonder if it was from the dishes. I just bought myself three dishes, bowls, sets of silver ware, and it was that big of a deal.

Thing you really NEED to replace are those listed above, toaster, wooden spoons (just switch to metal), any teflon surface (i just switched to aluminum pots/ pans), wooden cuting boards, and do a VERY thorough cleaning of the shelves and fridge. I would recommend keeping your food on one side of the kitchen and making it a habit it put down your gluten-free cutting board when you place any of your food on the counter. Even if you arent sensetive, if you have Celiac the external results are not the same as the internal-- meaning it might not be making you feel sick, but its still attacking your intestines.

Bea-- I have an aluminum pressure cooker too-- I think we should be ok with aluminum as long as there is no teflon. I havent used mine yet, but my impression was as long as it is a pure metal surface we should be good to go.

I hope it is OK to use the old pressure cooker as a pot. I am thinking of waiting to use it for a while however. Its old, and may have been bought used, so who knows what it was used for, though I haven't cooked glutenous items for many years. I have had this nasal congestion/throat irritation for over 2 1/2 weeks and just want to lose it. Am way better but still it drags on. So I thought, maybe its the old aluminum pot? I used it for chicken soup. I do have a stainless steel pot I trust more...

Bea

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Rejoicephd commented on Jefferson Adams's article in Gluten-Free Cooking
      1

      Your Complete Gluten-Free Thanksgiving Plan: Recipes, Tips & Holiday Favorites

    2. - marion wheaton replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?

    3. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?

    4. - BlessedinBoston replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,416
    • Most Online (within 30 mins)
      7,748

    Heather8280
    Newest Member
    Heather8280
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.